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Internal ID UUID643fd1d406ecc557263604
Scientific name Euryops lateriflorus
Authority (L.f.) DC.
First published in 394

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Synonyms Top

Scientific name Authority First published in
Jacobaeastrum lateriflorum Kuntze Revis. Gen. Pl. 1: 347 (1891)
Othonna lateriflora L.f. Suppl. Pl. : 387 (1782)
Jacobaeastrum subsessile Kuntze Revis. Gen. Pl. 1: 348 (1891)
Euryops pearsonii E.Phillips Ann. S. African Mus. ix. 346 (1917).
Euryops subsessilis Sch.Bip. Flora 28: 52 (1845)

Common names Top

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Language Common/alternative name
Afrikaans soetharpuisbos
Afrikaans harpuisbo
Afrikaans repuishout
Afrikaans vetharpuis

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000118551
Tropicos 2721342
KEW urn:lsid:ipni.org:names:207440-1
The Plant List gcc-79873
Open Tree Of Life 813654
NCBI Taxonomy 551061
IPNI 207440-1
iNaturalist 585725
GBIF 5395042
EPPO EYOLA

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Natürlich vorkommende Terpen‐Derivate, XXXIX. Über die Inhaltsstoffe der Gattung <i>Euryops</i> Ferdinand Bohlmann, Christa Zdero, Michael Grenz Wiley 29-Jun-2007
doi:10.1002/CBER.19741070835
Neue furanoeremophilane und andere sesquiterpene aus vertretern der gattung Euryops Ferdinand Bohlmann, Christa Zdero Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)94305-X

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(1S,2R,3S,4aR,5S,7S,8aR)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalene-1,2,7-triol 162846993 Click to see CC1CC(CC2C1(CC(C(C2O)O)C(=C)C)C)O 254.36 unknown https://doi.org/10.1002/CBER.19741070835
(2,7-dihydroxy-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-1-yl) 3-methylpent-2-enoate 327382 Click to see CCC(=CC(=O)OC1C2CC(CC(C2(CC(C1O)C(=C)C)C)C)O)C 350.50 unknown https://doi.org/10.1002/CBER.19741070835
(7-acetyloxy-2-hydroxy-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-1-yl) 2-methylbut-2-enoate 162947345 Click to see CC=C(C)C(=O)OC1C2CC(CC(C2(CC(C1O)C(=C)C)C)C)OC(=O)C 378.50 unknown https://doi.org/10.1016/S0031-9422(00)94305-X
https://doi.org/10.1002/CBER.19741070835
[(1S,2R,3R,4aR,5S,7S,8aR)-2,7-dihydroxy-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-1-yl] (Z)-3-methylpent-2-enoate 162866136 Click to see CCC(=CC(=O)OC1C2CC(CC(C2(CC(C1O)C(=C)C)C)C)O)C 350.50 unknown https://doi.org/10.1002/CBER.19741070835
[(1S,2R,3R,4aR,5S,7S,8aR)-2,7-dihydroxy-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-1-yl] 3-methylbut-2-enoate 24011689 Click to see CC1CC(CC2C1(CC(C(C2OC(=O)C=C(C)C)O)C(=C)C)C)O 336.50 unknown https://doi.org/10.1002/CBER.19741070835
[(1S,2R,3R,4aR,5S,7S,8aR)-7-acetyloxy-2-hydroxy-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-1-yl] (Z)-2-methylbut-2-enoate 162947346 Click to see CC=C(C)C(=O)OC1C2CC(CC(C2(CC(C1O)C(=C)C)C)C)OC(=O)C 378.50 unknown https://doi.org/10.1016/S0031-9422(00)94305-X
https://doi.org/10.1002/CBER.19741070835
Bohlmann K2604 327375 Click to see CC1CC(CC2C1(CC(C(C2OC(=O)C=C(C)C)O)C(=C)C)C)O 336.50 unknown https://doi.org/10.1002/CBER.19741070835

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